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Tetrabutylammonium phosphate monobasic

puriss., ≥99.0% (T)

Tetrabutylammonium dihydrogen phosphate
Linear Formula:
CAS Number:
Molecular Weight:
EC Number:
MDL number:
PubChem Substance ID:



Quality Level


≥99.0% (T)




151-154 °C (lit.)

SMILES string




InChI key


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General description

Tetrabutylammonium phosphate monobasic is a synthetic reagent.


Tetrabutylammonium phosphate monobasic is the suitable reagent used in the following studies:
  • Resolution of disaccharides reverse-phase ion-pairing HPLC (RPIP-HPLC).
  • Disaccharide analysis of 35S- heparan sulfate (HS).
  • As folding buffer for the dissolution of desalted oligonucleotides.
It may be used as reagent for the analysis of tetrasaccharides and 35S-disaccharides by HPLC. It may also be used in the preparation of monobasic tetrabutylammonium phosphate (TBAP) imprinted polymers.

Storage Class Code

13 - Non Combustible Solids



Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificate of Analysis

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Certificate of Origin

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More Documents

Quotes and Ordering

Robert D Gray et al.
Nucleic acids research, 36(12), 4191-4203 (2008-06-24)
Cation-induced folding into quadruplex structures for three model human telomeric oligonucleotides, d[AGGG(TTAGGG)(3)], d[TTGGG(TTAGGG)(3)A] and d[TTGGG(TTAGGG)(3)], was characterized by equilibrium titrations with KCl and NaCl and by multiwavelength stopped flow kinetics. Cation binding was cooperative with Hill coefficients of 1.5-2.2 in
Polymerisable squaramide receptors for anion binding and sensing.
Manesiotis P, et al.
Journal of Material Chemistry C, 2(42), 8990-8995 (2014)
Vaibhav Tiwari et al.
Journal of virology, 80(18), 8970-8980 (2006-08-31)
Herpes simplex virus type 1 (HSV-1) infection of the corneal stroma remains a major cause of blindness. Primary cultures of corneal fibroblasts (CF) were tested and found susceptible to HSV-1 entry, which was confirmed by deconvolution imaging of infected cells.
J Liu et al.
The Journal of biological chemistry, 274(53), 38155-38162 (1999-12-23)
3-O-Sulfation of glucosamine by heparan sulfate D-glucosaminyl 3-O-sulfotransferase (3-OST-1) is the key modification in anticoagulant heparan sulfate synthesis. However, the heparan sulfates modified by 3-OST-2 and 3-OST-3A, isoforms of 3-OST-1, do not have anticoagulant activity, although these isoforms transfer sulfate
Guoqing Xia et al.
The Journal of biological chemistry, 277(40), 37912-37919 (2002-07-26)
Heparan sulfate 3-O-sulfotransferase transfers sulfate to the 3-OH position of a glucosamine residue of heparan sulfate (HS) to form 3-O-sulfated HS. The 3-O-sulfated glucosamine residue contributes to two important biological functions of HS: binding to antithrombin and thereby carrying anticoagulant

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